Canonical Allele Identifier: CA399389713
Gene: KRT12 HGNC NCBI

Linked Data

dbSNP Id: rs1416567493
gnomAD v2: 17-39023372-A-T
gnomAD v4: 17-40867120-A-T
MyVariant Identifiers: chr17:g.39023372A>T (hg19) chr17:g.40867120A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867120A>T , CM000679.2:g.40867120A>T GRCh38
NC_000017.10:g.39023372A>T , CM000679.1:g.39023372A>T GRCh37
NC_000017.9:g.36276898A>T NCBI36
NG_008077.1:g.5091T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.67T>A MANE Select ENSP00000251643.4:p.Ser23Thr
ENST00000647902.1:c.67T>A ENSP00000497770.1:p.Ser23Thr
ENST00000251643.4:c.67T>A ENSP00000251643.4:p.Ser23Thr
NM_000223.3:c.67T>A NP_000214.1:p.Ser23Thr
XR_934754.1:n.1500+16260A>T
XR_934754.2:n.2008+16260A>T
NM_000223.4:c.67T>A MANE Select NP_000214.1:p.Ser23Thr
Search 100 bp 5'
Search 100 bp 3'